Canonical Allele Identifier: CA725611916

Gene: CYBA

Linked Data

• dbSNP Id: rs1297582592
• gnomAD v3: 16-88643310-TG-T
• gnomAD v4: 16-88643310-TG-T
• MyVariant Identifiers: chr16:g.88709719del (hg19) ; chr16:g.88643311del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88643311del , CM000678.2:g.88643311del	GRCh38
NC_000016.9:g.88709719del , CM000678.1:g.88709719del	GRCh37
NC_000016.8:g.87237220del	NCBI36
NG_007291.1:g.12739del , LRG_52:g.12739del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696156.1:c.*42del	ENSP00000512446.1:n.*42del
ENST00000696157.1:c.*847del	ENSP00000512447.1:n.*847del
ENST00000696158.1:c.*884del	ENSP00000512448.1:n.*884del
ENST00000696159.1:c.*553del	ENSP00000512449.1:n.*553del
ENST00000696160.1:c.*42del	ENSP00000512450.1:n.*42del
ENST00000696161.1:c.760del	ENSP00000512451.1:p.Gln254AsnfsTer?
ENST00000696162.1:c.*1349del	ENSP00000512452.1:n.*1349del
ENST00000696163.1:c.*42del	ENSP00000512453.1:n.*42del
ENST00000261623.8:c.*42del MANE Select	ENSP00000261623.3:n.*42del
ENST00000261623.7:c.*42del	ENSP00000261623.3:n.*42del
NM_000101.3:c.*42del	NP_000092.2:n.*42del
NM_000101.4:c.*42del MANE Select	NP_000092.2:n.*42del